Papers

Peer-reviewed Lead author Corresponding author
2014

Significant enhancement of photocatalytic activity of rutile TiO2 compared with anatase TiO2 upon Pt nanoparticle deposition studied by far-ultraviolet spectroscopy

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
  • Ichiro Tanabe
  • ,
  • Takayuki Ryoki
  • ,
  • Yukihiro Ozaki

Volume
16
Number
17
First page
7749
Last page
7753
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1039/c4cp00329b
Publisher
ROYAL SOC CHEMISTRY

Absorption spectra of anatase and rutile TiO2 in the 150-300 nm region before and after the deposition of Pt nanoparticles were measured. For anatase TiO2, the spectral intensity in the longer wavelength region decreased (>similar to 210 nm), while that in the shorter wavelength region increased (<similar to 210 nm). In particular, spectral band intensity in the far-ultraviolet (FUV) region (similar to 160 nm) was increased. In contrast, the spectral intensity of rutile TiO2 increased over the entire wavelength region under investigation. Rutile TiO2 showed a spectral band at a longer wavelength region (similar to 170 nm) than anatase TiO2, and the difference in the band wavelengths in the FUV region was due to the differences in the electronic structures of their phase. The decrease and increase in the intensity upon the Pt nanoparticle deposition suggest electron transfer from the TiO2 to Pt nanoparticles and enhancement of charge-separation, respectively. The photocatalytic activity of rutile TiO2, as evaluated by a photo-degradation reaction of methylene blue, increased more than that of anatase TiO2 upon the deposition of Pt nanoparticles. Thus, we concluded that the charge-separation efficiency of rutile TiO2 is enhanced relative to that of anatase TiO2 upon the deposition of Pt nanoparticles.

Link information
DOI
https://doi.org/10.1039/c4cp00329b
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000334200400014&DestApp=WOS_CPL
ID information
  • DOI : 10.1039/c4cp00329b
  • ISSN : 1463-9076
  • eISSN : 1463-9084
  • Web of Science ID : WOS:000334200400014

Export
BibTeX RIS